首页> 外文期刊>Liver international : >Hepatic steatosis in patients with chronic hepatitis C virus genotype 2 or 3 does not affect viral response in patients treated with peginterferon alpha-2a (40KD) (PEGASYS) plus ribavirin (COPEGUS) for 16 or 24 weeks.
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Hepatic steatosis in patients with chronic hepatitis C virus genotype 2 or 3 does not affect viral response in patients treated with peginterferon alpha-2a (40KD) (PEGASYS) plus ribavirin (COPEGUS) for 16 or 24 weeks.

机译:患有慢性丙型肝炎病毒基因型2或3的患者的肝脂肪变性不会影响接受聚乙二醇干扰素α-2a(40KD)(PEGASYS)加利巴韦林(COPEGUS)治疗16周或24周的病毒反应。

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BACKGROUND: Hepatic steatosis is common in patients infected with hepatitis C virus (HCV). The effect of steatosis on anti-HCV therapy efficacy is unclear. METHODS: We studied host and viral factors associated with steatosis and the effect of steatosis on treatment efficacy using the database of a large prospective trial in patients with HCV genotypes 2 and 3. RESULTS: Out of 885 patients assessed for steatosis, a total of 614 patients or 69% had steatosis. Patients with genotype 3 were more likely to have steatosis than those with genotype 2 (79 vs. 59%, P<0.001). Using the logistic regression model, steatosis was associated with genotype 3 (P<0.0001), older age (P=0.0025), heavier weight (P<0.0001), higher HCV RNA (P<0.0001), and higher ALT levels (P=0.015). By univariate analysis, steatosis was associated with lower sustained virological response (SVR) in patients with genotype 3, but not in patients with genotype 2. When all factors associated with steatosis and SVR were evaluated by logistic regression analysis; genotype, age, bodyweight, histological diagnosis, ALT quotient, baseline HCV RNA and treatment duration were associated with the probability of SVR, but gender, race and steatosis were not. Further analysis showed that steatosis remained a non-significant factor while baseline viral load was significantly associated with the probability of an SVR. CONCLUSIONS: Steatosis did not influence the efficacy of treatment in our study population. Baseline viral load is a confounding factor, particularly in patients infected with genotype 3 and once baseline viral load was accounted for, the association between steatosis and SVR was not relevant.
机译:背景:肝脂肪变性在感染丙型肝炎病毒(HCV)的患者中很常见。脂肪变性对抗HCV治疗功效的影响尚不清楚。方法:我们使用一项大型前瞻性试验的数据库对2型和3型HCV患者进行了研究,研究了与脂肪变性相关的宿主和病毒因素以及脂肪变性对治疗效果的影响。结果:在885例评估脂肪变性的患者中,共有614例患者或69%患有脂肪变性。基因型3的患者比基因型2的患者更有可能发生脂肪变性(79%vs. 59%,P <0.001)。使用logistic回归模型,脂肪变性与基因型3(P <0.0001),年龄较大(P = 0.0025),体重较重(P <0.0001),HCV RNA较高(P <0.0001)和ALT水平较高(P = 0.015)。通过单因素分析,脂肪变性与基因型3的患者的持续病毒学应答(SVR)较低相关,而与基因型2的患者无关。当通过逻辑回归分析评估与脂肪变性和SVR相关的所有因素时,脂肪变性与基因型2的患者无关。基因型,年龄,体重,组织学诊断,ALT商,基线HCV RNA和治疗持续时间与SVR发生率相关,而性别,种族和脂肪变性则不相关。进一步的分析表明,脂肪变性仍然是不重要的因素,而基线病毒载量与SVR的可能性显着相关。结论:脂肪变性没有影响我们研究人群的治疗效果。基线病毒载量是一个混杂因素,尤其是在感染了基因型3的患者中,一旦考虑了基线病毒载量,脂肪变性和SVR之间的关联就不相关了。

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